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Vorinostat

ZOLINZA

Pronunciation: vor-IN-oe-stat (zoe-LINZ-a)

Vorinostat ballicule: receptor binding, kinetics and half-life diagram
Mechanism of action: Vorinostat ballicule

What it isHistone deacetylase inhibitor; cutaneous T-cell lymphoma.

Why this oneOral epigenetic therapy for a disease with few systemic options.

What limits itThrombocytopenia, fatigue and QT prolongation. Dehydration from GI losses is common.

Vorinostat molecular structure (skeletal formula)
Molecular structure: Vorinostat

FDA-approved for

FDA label

FDA dosingPopulationStartTargetMax
Cutaneous T-cell lymphoma (CTCL)adult400 mg QD400 mg QD400 mg QD

Renal Undefined

Hepatic Mild-moderate (bilirubin 1-3×ULN or AST>ULN): reduce to 300 mg QD; severe: insufficient data

For intolerance, may reduce to 300 mg QD, then 300 mg QD for 5 consecutive days/week

Instructions

Available strengths

Cautions

Adverse reactions

Pregnancy Can cause fetal harm; advise of potential risk to fetus

Lactation Do not breastfeed during and for ≥1 week after last dose

Cost

Vorinostat (ZOLINZA)
Strength#/mogeneric $/moCostPlus
100 mgcap30 qdnot offered
NADAC is a voluntary CMS survey of what retail community pharmacies pay for the drugs they stock. Vorinostat is dispensed outside retail pharmacies, so it rarely appears on surveyed invoices.

Generic entry2027 est.

NO BOXED WARNINGS

Principal riskThrombocytopenia and QT prolongation

Classes and tags

Clinical profile

Therapeutic safety burden3 / 4
Overdose danger2 / 4
Weight-gain liability0 / 4
Sedation liability0 / 4
QT / Torsades0 / 4
Direct muscarinic antagonism0 / 4
Embryofetal risk3 / 4

Legacy pregnancy categoryD

Defining liabilityMyelosuppression and agent-specific hepatic, cardiac, pulmonary, neurologic or reproductive toxicity require oncology monitoring.

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